Reacción #1605773

ord-9332be9bf76d476dacd2441d061bee3e

Ecuación de reacción

O
water
Cl
HCl
COc1cc(C)ccc1C(N)=O
2-methoxy-4-methylbenzamide
B.C1CCOC1
Borane tetrahydrofuran
COc1cc(C)ccc1CN
(2-methoxy-4-methylphenyl)methanamine
Rendimiento 64.0%

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction was cooled to room temperature
  2. 2
    Temperaturathe reaction mixture was then heated at 70° C. for 2 hrs
  3. 3
    TemperaturaAfter cooling
  4. 4
    Lavadothe resulting solution was washed with ether
  5. 5
    Otrowas basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3
  6. 6
    Extracciónthen extracted with ethyl acetate
  7. 7
    LavadoThe organic layer was washed with brine
  8. 8
    Secadodried over MgSO4
  9. 9
    Filtraciónfiltered
  10. 10
    Otroevaporated

Procedimiento

To a solution of 2-methoxy-4-methylbenzamide (14.55 g, 88.08 mmol) in dry THF (50 mL) was added dropwise Borane-tetrahydrofuran complex (1.0 M in THF, 220 mL, 2.5 eq) at 0° C. under N2 atmosphere. The reaction mixture was then heated to 60° C. overnight. The reaction was cooled to room temperature, aq.HCl (6 N, 37 mL) was added carefully and the reaction mixture was then heated at 70° C. for 2 hrs. After cooling, water was added and the resulting solution was washed with ether. The aqueous layer was basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3 then extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated to give 8.5 g of (2-methoxy-4-methylphenyl)methanamine. (64% yield)

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09072313B2uspto-grants-2015_07